Primary Device ID | 00810093080014 |
NIH Device Record Key | 9cee3b95-c13d-4e77-be36-6883d59756cb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PainPod |
Version Model Number | JQ-5C-07A |
Company DUNS | 124034476 |
Company Name | Hi-Dow International Incorporated |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810093080014 [Primary] |
NUH | Stimulator, Nerve, Transcutaneous, Over-The-Counter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-05-24 |
Device Publish Date | 2022-05-16 |
00799439774025 | PainPod III |
00799439774018 | PainPod XPV |
09351609000023 | PainPod Mi |
00851640007511 | Electronic Muscle Stimulator white |
00810093080014 | TENS for pain relief |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PAINPOD 87820529 not registered Dead/Abandoned |
Dannemiller, Inc. 2018-03-05 |
PAINPOD 86155069 4657624 Live/Registered |
HIDOW GROUP PTY LTD 2013-12-31 |
PAINPOD 85593309 not registered Dead/Abandoned |
Pinook USA, LLC 2012-04-10 |